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510(k) Data Aggregation

    K Number
    K170055

    Validate with FDA (Live)

    Manufacturer
    Date Cleared
    2017-04-13

    (97 days)

    Product Code
    Regulation Number
    888.3060
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The CAPRI Corpectomy Cage System is a vertebral body replacement device intended for use in the thoracolumbar spine (T1 to L5) to replace collapsed, damaged, or unstable vertebral bodies due to tumor or trauma (i.e., fracture). The CAPRI Corpectomy Cage System is designed to provide anterior spinal column support even in the absence of fusion for a prolonged period. The CAPRI device may be used with allograft or autograft.

    For all the above indications the CAPRI implants are intended to be used with supplemental internal fixation appropriate for the implanted level, including K2M Pedicle Screw and Hook Systems, and K2M Spinal Plate Systems.

    Device Description

    The CAPRI Corpectomy System implants are vertebral body replacement devices that are designed in a variety of lengths, widths and heights to match the patient's anatomy. Solid (titanium alloy) and adjustable (titanium alloy and cobalt chrome) cages are available and can be implanted via posterior, anterior or lateral approaches. The implants of the CAPRI Corpectomy Cage Systems are manufactured from Titanium alloy (per ASTM F3001) and Cobalt Chrome (per ASTM F1537).

    Function: The system is used to provide structural stability in skeletally mature individuals following a corpectomy or vertebrectomy.

    AI/ML Overview

    This document is a 510(k) summary for the CAPRI Corpectomy Cage System, a medical device for vertebral body replacement. It details the device's intended use, classification, technological comparison to predicate devices, and non-clinical performance evaluation. It does not contain information about clinical acceptance criteria or studies with human subjects.

    Therefore, I cannot provide the requested information, which pertains to clinical acceptance criteria, device performance on a test set, expert involvement, or human reader effectiveness studies. The document only describes non-clinical mechanical testing.

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